4.5 Article

Analogues of muramyl dipeptide (MDP) and tuftsin limit infection and inflammation in murine model of sepsis

期刊

VACCINE
卷 27, 期 3, 页码 369-374

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.vaccine.2008.11.017

关键词

Sepsis; Muramyl dipeptide; Tuftsin

资金

  1. Polish State Committee for Scientific Research [2 PO5A 004 28, N N401 217534]
  2. Iceland, Liechtenstein
  3. European Economic Area Financial Mechanism Office

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Pharmacological manipulation of the balance between pro-and anti-inflammatory mediators emerges as a key aspect of a successful treatment of sepsis. A murine model of septic shock was developed and chosen conjugates (1a, 1b, 8a, 8c) and analogs (T2) of muramyl dipeptide and tuftsin were tested in this model as prospective anti-bacterial drugs or adjuvants. The phagocytic activity of monocytes/macrophages was determined (flow cytometry, bacterial clearance from vital organs). To evaluate cytokines levels (TNF alpha, IFN gamma, IL6, IL10) we used real-time PCR. The most promising immunomodulatory properties were displayed by the analogue T2 and two conjugates: 8a, 8c. (C) 2008 Elsevier Ltd. All rights reserved.

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